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KD-Validated Anti-TIA1 Rabbit Monoclonal Antibody #62711

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Flow cytometric analysis of TIA1 expression in HAP-1 cells using anti-TIA1 antibody (Cat#62711, 1:2,000). Green, isotype control; red, TIA1.
Immunocytochemical staining of HAP1 cells with anti-TIA1 antibody (Cat#62711, 1:1,000) . Nuclei were stained blue with DAPI; TIA1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar, 20 μm.
Western blotting analysis using anti-TIA1 antibody (Cat#62711). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-TIA1 antibody (Cat#62711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-TIA1 antibody (Cat#62711). TIA1 expression in wild-type (WT) and TIA1 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-TIA1 antibody (Cat#62711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HeLa cells using anti-TIA1 antibody (Cat#62711, 1:1,000), Top panel: wild-type (WT); Bottom panal: TIA1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; TIA1 was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm. Permeabilization: Triton.
  • 基因名：
    TIA1
  • 货号：
    62711
  • 应用：
    WB, FCM, IC
  • 物种反应性：
    H, M, R
规格：
20 μL，50 μL，100 μL
价格：
¥ 650.00，¥ 1,350.00，¥ 2,500.00

Information

Picture

Citation(0)

Information
Product Name KD-Validated Anti-TIA1 Rabbit Monoclonal Antibody
Aliases TIA1; TIA1 Cytotoxic Granule Associated RNA Binding Protein; TIA-1; T-Cell-Restricted Intracellular Antigen-1; Cytotoxic Granule Associated RNA Binding Protein TIA1; Nucleolysin TIA-1 Isoform P40; TIA1 Cytotoxic Granule-Associated RNA-Binding Protein; P40-TIA-1 (Containing P15-TIA-1); RNA-Binding Protein TIA-1; P40-TIA-1; ALS26; WDM
Background

Gene Name: TIA1

NCBI Gene Entry: 7072

UniProt Entry: P31483
Application Information

Molecular Weight: Predicted, 43 kDa, observed, 43 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 24GB2175

Species Reactivity: Human, mouse, rat

Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (IC)
Immunogen A synthesized peptide derived from human TIA1
Isotype Rabbit IgG
Storage Buffer Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
Storage Store at -20 °C for one year.
Recommended Dilutions Western Blotting (WB): 1:1,000-1:5,000
Flow Cytometry (FCM): 1:2,000
Immunocytochemistry (IC): 1:100-1:1,000
Note This product is for research use only.
Picture
  • Flow cytometric analysis of TIA1 expression in HAP-1 cells using anti-TIA1 antibody (Cat#62711, 1:2,000). Green, isotype control; red, TIA1.
  • Immunocytochemical staining of HAP1 cells with anti-TIA1 antibody (Cat#62711, 1:1,000) . Nuclei were stained blue with DAPI; TIA1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar, 20 μm.
  • Western blotting analysis using anti-TIA1 antibody (Cat#62711). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-TIA1 antibody (Cat#62711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Western blotting analysis using anti-TIA1 antibody (Cat#62711). TIA1 expression in wild-type (WT) and TIA1 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-TIA1 antibody (Cat#62711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
  • Immunocytochemical staining of HeLa cells using anti-TIA1 antibody (Cat#62711, 1:1,000), Top panel: wild-type (WT); Bottom panal: TIA1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; TIA1 was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm. Permeabilization: Triton.
Citation(0)
  • 基因名：
    TIA1
  • 货号：
    62711
  • 应用：
    WB, FCM, IC
  • 物种反应性：
    H, M, R
规格：
20 μL，50 μL，100 μL
价格：
¥ 650.00，¥ 1,350.00，¥ 2,500.00
RELATED PRODUCTS
Flow cytometric analysis of TIA1 expression in HAP-1 cells using anti-TIA1 antibody (Cat#62711, 1:2,000). Green, isotype control; red, TIA1.
Immunocytochemical staining of HAP1 cells with anti-TIA1 antibody (Cat#62711, 1:1,000) . Nuclei were stained blue with DAPI; TIA1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar, 20 μm.
Western blotting analysis using anti-TIA1 antibody (Cat#62711). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-TIA1 antibody (Cat#62711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-TIA1 antibody (Cat#62711). TIA1 expression in wild-type (WT) and TIA1 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-TIA1 antibody (Cat#62711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HeLa cells using anti-TIA1 antibody (Cat#62711, 1:1,000), Top panel: wild-type (WT); Bottom panal: TIA1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; TIA1 was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm. Permeabilization: Triton.
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